Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Type Device Class Implantable

Show Filters

Filters are currently being applied
Single Action Persuader
Seaspine Orthopedics Corporation
SR-0314
Not in Commercial Distribution

  • 10889984163072 ()
SR-0314

  • Orthopaedic rod reducer
MIS ROD, PRECONTOURED, 6.0 x 150mm
Seaspine Orthopedics Corporation
MM1-176150
In Commercial Distribution

  • 10889981440022 ()
MM1-176150

  • Bone-screw internal spinal fixation system rod
Double Barrel DTS Guide 0°
Seaspine Orthopedics Corporation
SR-1388
In Commercial Distribution

  • 10889981437572 ()
SR-1388

  • Surgical drill guide, reusable
Universal Lid, 10x10, Orthofix Orange
Seaspine Orthopedics Corporation
ST3-000013
In Commercial Distribution

  • 10889981437527 ()
ST3-000013

  • Instrument tray, reusable
Cross-Connector Tray Base
Seaspine Orthopedics Corporation
MD3-210001
In Commercial Distribution

  • 10889981437510 ()
MD3-210001

  • Instrument tray, reusable
Inline Reducer, Robust
Seaspine Orthopedics Corporation
SR-1373
In Commercial Distribution

  • 10889981435592 ()
SR-1373

  • Orthopaedic rod reducer
Double Barrel DTS Guide 15°
Seaspine Orthopedics Corporation
SR-1367
In Commercial Distribution

  • 10889981434632 ()
SR-1367

  • Surgical drill guide, reusable
Angled No-Profile Lock Inserter
Seaspine Orthopedics Corporation
SR-1340
In Commercial Distribution

  • 10889981427191 ()
SR-1340

  • Orthopaedic inorganic implant inserter/extractor, reusable
Anterior Plate Inserter
Seaspine Orthopedics Corporation
SR-1342
In Commercial Distribution

  • 10889981427092 ()
SR-1342

  • Orthopaedic inorganic implant inserter/extractor, reusable
Lateral DTS Guide, 15 Deg
Seaspine Orthopedics Corporation
AP2-100125
In Commercial Distribution

  • 10889981276874 ()
AP2-100125

  • Surgical drill guide, reusable
< 1 2 3 4 5 ... 190 >

Having trouble finding the UDI and/or device in GUDID? Send a picture of the label to GUDIDSupport@fda.hhs.gov.